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Surgical Guide for Carbon

FDA UDI

Class I (US FDA UDI)

by Whip-Mix Corp.

Identity

Trade Name
Surgical Guide for Carbon FDA UDI
Generic Name
Custom-made orthopaedic/craniofacial surgical guide FDA UDI
Device Name
Accessories, Implant, Dental, Endosseous FDA UDI
Model / Reference
71079-C FDA UDI
Description
Accessories, Implant, Dental, Endosseous FDA UDI

Identifiers

Primary DI / UDI-DI
D04071079C1 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Custom-made orthopaedic/craniofacial surgical guide FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Custom-made orthopaedic/craniofacial surgical guide

Surgical Guide for Carbon by Whip-Mix Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Custom-made orthopaedic/craniofacial surgical guide.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Whip-Mix Corp.

Sources (1)

  • FDA UDI 17b2518e-f751-4577-82b7-cff1c6e4ce0a 33 fields · synced May 30, 2026